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rs199473108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473108(C;G)
Make rs199473108(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606071
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473108
ebirs199473108
HLIrs199473108
Exacrs199473108
Varsomers199473108
Maprs199473108
PheGenIrs199473108
hapmaprs199473108
1000 genomesrs199473108
hgdprs199473108
ensemblrs199473108
gopubmedrs199473108
geneviewrs199473108
scholarrs199473108
googlers199473108
pharmgkbrs199473108
gwascentralrs199473108
openSNPrs199473108
23andMers199473108
23andMe allrs199473108
SNP Nexus

SNPshotrs199473108
SNPdbers199473108
MSV3drs199473108
GWAS Ctlgrs199473108
Max Magnitude0
ClinVar
Risk rs199473108(A,G,T;A,G,T)
Alt rs199473108(A,G,T;A,G,T)
Reference rs199473108(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38647562G>C; NC_000003.11:g.38647562G>T
CLNSRC ClinVar
CLNACC RCV000058406.2, RCV000058405.2, RCV000182963.2,